Source: BEFREE ×
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs118101777
rs118101777
IDH2
42 0.614 0.280 15 90087472 missense variant C/T snv 2.0E-03 1.6E-03 0.010 1.000 1 2016 2016
dbSNP: rs121913273
rs121913273
PIK3CA
22 0.605 0.440 3 179218294 missense variant G/A;C snv 0.010 1.000 1 2019 2019
dbSNP: rs121913500
rs121913500
IDH1
83 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 2016 2016
dbSNP: rs121913503
rs121913503
IDH2
18 0.689 0.200 15 90088606 missense variant C/A;T snv 0.010 1.000 1 2016 2016